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Functional characterization of the human myosin-7a motor domain
Myosin-7a participates in auditory and visual processes. Defects in MYO7A, the gene encoding the myosin-7a heavy chain, are causative for Usher syndrome 1B, the most frequent cause of deaf-blindness in humans. In the present study, we performed a detailed kinetic and functional characterization of t...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SP Birkhäuser Verlag Basel
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249170/ https://www.ncbi.nlm.nih.gov/pubmed/21687988 http://dx.doi.org/10.1007/s00018-011-0749-8 |